What is NDC 23155-920?

23155-920 is the product NDC for Amlodipine and Benazepril Hydrochloride, Amlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1 capsule, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

What is the active ingredient?

Amlodipine besylate, Benazepril hydrochloride.

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Amlodipine and Benazepril Hydrochloride?

39 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Amlodipine and Benazepril Hydrochloride NDC 23155-920

NDC codes

FDA NDC Directory

Product NDC (as listed)23155-920Labeler and product segments. Claims need a package NDC.

Product NDC at billing width23155-0920Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
23155-920-01	23155092001	100 CAPSULE in 1 BOTTLE (23155-920-01)Marketed from Dec 19, 2025
23155-920-05	23155092005	500 CAPSULE in 1 BOTTLE (23155-920-05)Marketed from Dec 19, 2025
23155-920-10	23155092010	1000 CAPSULE in 1 BOTTLE (23155-920-10)Marketed from Dec 19, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Amlodipine and Benazepril Hydrochloride
Generic name (nonproprietary): amlodipine and benazepril hydrochloride
Active ingredients: Amlodipine besylate — 2.5 mg/1Benazepril hydrochloride — 10 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.NDC labeler code 23155
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091431
Marketing start: Dec 19, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)Dihydropyridines (Chemical structure)
Identifiers: Product ID 23155-920_ecbe2177-2319-4e49-a47a-48dd1aefe99fSPL ID ecbe2177-2319-4e49-a47a-48dd1aefe99fSPL set ID 27b0c628-820a-48bf-a411-86c0ebd4cc8dRxCUI 898342, 898346, 898350, 898353, 898356, 898359UNII 864V2Q084H, N1SN99T69TUPC 0323155923100, 0323155921052, 0323155924107, 0323155925012, 0323155920109, 0323155922059, 0323155924053, 0323155921014, 0323155924015, 0323155925104, 0323155920017, 0323155922103, 0323155921106, 0323155925050, 0323155920055, 0323155923018, 0323155923056, 0323155922011
Pharmacologic class: Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N423155092001 followed by a unit qualifier and the quantity

Package 23155-0920-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jun 29, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Amlodipine and benazepril hydrochloride capsules are a combination capsule of amlodipine, a dihydropyridine calcium channel blocker (DHP CCB) and benazepril, an angiotensin-converting enzyme (ACE) inhibitor. Amlodipine and benazepril hydrochloride capsules are indicated for the treatment of hypertension in patients not adequately controlled on monotherapy with either agent. (1) 1.1 Hypertension Amlodipine and benazepril hydrochloride capsules are indicated for the treatment of hypertension in patients not adequately controlled on monotherapy with either agent.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23155-920

What is NDC 23155-920?: 23155-920 is the product NDC for Amlodipine and Benazepril Hydrochloride, Amlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1 capsule, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Amlodipine and Benazepril Hydrochloride.
What is the active ingredient?: Amlodipine besylate, Benazepril hydrochloride.
Who is the labeler?: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Amlodipine and Benazepril Hydrochloride?: 39 other product NDCs are listed under this name. See all Amlodipine and Benazepril Hydrochloride NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Amlodipine and Benazepril Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-923	23155-0923-0123155-0923-0523155-0923-10
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-924	23155-0924-0123155-0924-0523155-0924-10
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-921	23155-0921-0123155-0921-0523155-0921-10
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-922	23155-0922-0123155-0922-0523155-0922-10
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-925	23155-0925-0123155-0925-0523155-0925-10
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-8454	68788-8454-03
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Northwind Health Company, LLC	51655-213	51655-0213-2651655-0213-52
Amlodipine And Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	DIRECT RX	72189-260	72189-0260-90
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-1928	70518-1928-00
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	84677-008	84677-0008-01

All 40 Amlodipine and Benazepril Hydrochloride NDCs

Other NDCs under ANDA 091431

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 091431
Product	Strength	Form · route	Labeler	Product NDC
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-921
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-922
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-923
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-924
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-925
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	84677-008
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	84677-009
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	84677-010
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	84677-011
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	84677-012
Amlodipine and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	84677-013